EFFICIENCY REQUIREMENTS FOR NEW HOT-WATER BOILERS FIRED WITH LIQUID OR GASEOUS FUELS (IMPLEMENTING
Table of Provisions (10)
Statutory Text (10 Articles)
(IMPLEMENTING MEASURES)
SUBSIDIARY LEGISLATION 427.17
EFFICIENCY REQUIREMENTS FOR NEW
HOT-WATER BOILERS FIRED WITH LIQUID
OR GASEOUS FUELS (IMPLEMENTING
MEASURES) REGULATIONS
11th August, 2007
LEGAL NOTICE 348 of 2007.
(1) The title of these regulations is the Efficiency
Requirements for New Hot-Water Boilers Fired with Liquid or
Gaseous Fuels (Implementing Measures) Regulations.
(2) These regulations shall be interpreted in terms of the
Framework for the Setting of Ecodesign Requirements for Energy-
Using Products Regulations, hereinafter referred to as "the
Ecodesign Regulations".
(3)
(a) These regulations implement the requirements of
Council Directive 92/42/EEC * of 21 May 1992 on
efficiency requirements for new hot-water boilers fired
with liquid or gaseous fuels as amended by
(i)
Directive 2004/8/EC on the promotion of
cogeneration based on a useful heat demand in
the internal energy market and amending
Directive 92/42/EEC and,
(ii) Directive 2005/32/EC of the European
Parliament and of the Council of 6th July 2005
Establishing a Framework for the Setting of
Ecodesign Requirements for Energy-Using
Products and amending Council Directive 92/42/
EEC and Directives 96/57/EC † and 2000/55/EC ‡
of the European Parliament and of the Council.
(b) Council Directive 92/42/EEC falls under the SAVE
programme concerning the promotion of energy
efficiency in the Community.
(4) These regulations constitute an implementing measure with
in the meaning of the principal regulations with regard to energy
efficiency during use of boilers.
(1) These
regulations
determine
the
efficiency
requirements applicable to new hot-water boilers fired by liquid or
gaseous fuels with a rated output of no less than 4 kW and no more
than 400 kW, hereinafter called "boilers".
*OJ No. L167, 22-06-1992, p. 17-28
†OJ No. L236, 18-09-1996, p. 36-43
‡OJ No. L279, 01-11-2000, p. 33-39
(IMPLEMENTING MEASURES)
(2) The following shall be excluded from the scope of these
regulations
(a) hot-water boilers capable of being fired by different
fuels including solid fuels,
(b) equipment for the instantaneous preparation of hot
water,
(c) boilers designed to be fired by fuels the properties of
which differ appreciably from the properties of the
liquid and gaseous fuels commonly marketed
(industrial waste gas, biogas, etc),
(d) cookers and appliances designed mainly to heat the
premises in which they are installed and, as a
subsidiary function, to supply hot water for central
heating and sanitary hot water,
(e) appliances with rated outputs of less than 6 kW using
gravity circulation and designed solely for the
production of stored sanitary hot water,
(f)
appliances with rated outputs of less than 6 kW using
gravity circulation and designed solely for the
production of stored sanitary hot water,
(g) boilers manufactured on a one-off basis,
(h) cogeneration units as defined in Directive 2004/8/EC
of the European Parliament and of the Council of 11
February 2004 on the promotion of cogeneration based
on useful heat demand in the internal energy market * .
For the purposes of these regulations, the definitions of the
Ecodesign Regulations as well as the following definitions shall
apply
"appliance" means the boiler body designed to have a burner
fitted, or the burner designed to be fitted to a boiler body;
"average temperature of the boiler water" means the average of
the water temperatures at the entry and exit of the boiler;
"back-boiler" means a boiler designed to supply a central-heating
system and to be installed in a fireplace recess as part of a back
boiler/gas fire combination;
"boiler" means the combined boiler body-burner unit, designed
to transmit to water the heat released from burning;
"boiler to be installed in the living space" means a boiler with an
effective rated output of less than 37 kW, designed to provide heat
to the part of the living space in which it is installed by means of
the emission of heat from the casing having an open expansion
chamber, supplying hot water using gravity circulation; such
boilers shall bear on their casings the explicit indication that they
*L.N. 52 of 1996 : Appliances Burning Gaseous Fuels, implementing Directive 90/
396/EEC (OJ No. L 196, 26.07.90, p. 15-29).
(IMPLEMENTING MEASURES)
must be installed in living space;
"effective rated output (expressed in kW)" means the maximum
calorific output laid down and guaranteed by the manufacturer as
being deliverable during continuous operation while complying
with the useful efficiency indicated by the manufacturer;
"gas condensing boiler" means a boiler designed to condense
permanently a large part of the water vapour contained in the
combustion gases;
"low-temperature boiler" means a boiler which can work
continuously with a water supply temperature of 35 to 40°C,
possib ly produ cin g co nden satio n i n c ertai n circ um st ances,
including condensing boilers using liquid fuel;
"part load (expressed in %)" means the ratio between the
effective output of a boiler operating intermittently or at an output
lower than the effective rated output and the same effective rated
output;
"standard boiler" means a boiler for which the average water
temperature can be restricted by design;
"useful efficiency (expressed in %)" means the ratio between the
heat output transmitted to the boiler water and the product of the
net calorific value at constant fuel pressure and the consumption
expressed as a quantity of fuel per unit time.
(1) With regard to placing on the market and putting into
service mentioned in the principal regulations the following shall
apply
(a) boilers shall satisfy the efficiency requirements set out
in Schedule I, section 1, and the conditions for entry
into service laid down on the basis of local climatic
conditions and the energy and the occupancy
characteristics of the buildings;
(b) however, where back-boilers and, or boilers that are to
be installed in the living space are widely installed at
the date of the adoption of the Efficiency
Requirements for New Hot-Water Boilers Fired with
Liquid or Gaseous Fuels Regulations, 2002 * , the Malta
Standards Authority shall authorise their entry into
service, provided that their efficiency both at rated
output and at 30% part load is not more than 4% below
the requirements laid down in Schedule I, section 1,
for standard boilers;
(c) in the case of boilers with a dual function, that of
heating premises and also providing sanitary hot
water, the efficiency requirements referred to in
Schedule I, section 1, concern the heating function
only;
(d) where
boilers
are
subject
to
other
regulations
*Legal Notice 62 of 2002, revoked by these regulations.
(IMPLEMENTING MEASURES)
concerning other aspects which also provide for the
affixing of the ‘CE’ marking, the latter shall indicate
that the boilers in question are also presumed to
conform to the provisions of those regulations.
(2) Where one or more of these regulations allow the
manufacturer, during a transitional period, to choose which
arrangements to apply, the CE marking shall indicate conformity to
the provisions only of those regulations applied by the
manufacturer. In this case, particulars of the regulations applied, as
published in the OJ, must be given in the documents, notices or
instructions required by the regulations and accompanying the
boilers.
(1) With regard to the conformity assessment procedures
mentioned in the Ecodesign regulations the conformity of series-
produced boilers shall be certified by
(a) the examination of the efficiency of a boiler type in
accordance with module B as described in Schedule II,
and
(b) a declaration of conformity to the approved type in
accordance with module C, D or E as described in
Schedule III.
For boilers burning gaseous fuels, the procedures for
assessing the conformity of their efficiency shall be those used to
assess conformity to the safety requirements laid down in Directive
90/396/EEC4 on the approximation of the laws of the Member
States relating to appliances burning gaseous fuels.
(2) Where appliances marketed separately are placed on the
market, they must bear the CE marking and be accompanied by the
declaration of conformity, which defines the parameters enabling
them after assembly to achieve the useful efficiency levels laid
down in Schedule I.
With regard to notified bodies mentioned in the Ecodesign
Regulations a notified body shall also fulfil the criteria listed in
Schedule IV.
(IMPLEMENTING MEASURES)
Schedule I
Based on Article 5 of directive 92/42/EC
THE EFFICIENCY REQUIREMENTS
1. Boilers must comply with the following useful efficiency requirements
at rated output, i.e. operating at rated output Pn expressed in kW, at an
average boiler-water temperature of 70°C , and
a part load, i.e. operating at 30% part load, at an average boiler-water
temperature which varies according to the type of the boiler.
The useful efficiency requirements to be complied with are set out in the
following table
Type of boiler
Range of
Efficiency at rated output
Efficiency at part load
power output
Average
Efficiency
Average
Efficiency
boiler-water
requirement
boiler-water
requirement
kw
temperature
expressed
temperature
expressed
(in ºC)
(in %)
(in ºC)
(in %)
≥ 84 + 2 logPn
≥ 50
≥ 80 + 3 logPn
Standard boilers
4 to 400
≥ 87.5 + 1.5
≥ 87.5 + 1.5
Low-temperature
4 to 400
boilers(*)
logPn
logPn
≥ 91 + 1 logPn
≥ 97 + 1 logPn
Gas condensing boilers
4 to 400
30(**)
Including condensing boilers using liquid fuels.
Temperature of boiler water-supply.
2. The harmonized standards relating to the requirements of these regulations
drawn up under mandate from the Commission in accordance with Directive 83/189/
EEC * and 88/182/EEC † shall determine, inter alia, the verification methods valid for
production and measurements.
Appropriate tolerances must be incorporated in the efficiency levels.
Schedule II
Based on Annex III of Directive 92/42/EC
EC-TYPE EXAMINATION
Module B: EC type-examination
1. This module describes that part of the procedure by which a notified body
ascertains and attests that an example, representative of the production envisaged,
meets the relevant provisions of these regulations.
2. The application for EC type-examination is lodged by the manufacturer or
his authorized representative with a notified body of his choice.
The application must include
the name and address of the manufacturer and, if the application is
lodged by the authorized representative, the name and address in
addition,
*OJ No. L 109, 26.04.83, P. 08-12.
†OJ No. L 81, 26.03.88, P. 75.
(IMPLEMENTING MEASURES)
-
a written declaration that the same application has not been lodged with
any other notified body,
-
the technical documents, as described in section 3 of this Module.
The applicant must place at the disposal of the notified body an example
representative of the production envisaged, hereinafter called ‘type’. The notified
body may request further examples if needed for carrying out the test programme.
3. The technical documents must enable the conformity of the appliance with
the requirements of these regulations to be assessed. They must, as far as is relevant
for such assessment, cover the design, manufacture and operation of the appliance
and contain as far as is relevant for assessment
-
a general type-description,
-
conceptual design and manufacturing drawings and diagrams of
components, sub-assemblies, circuits, etc.,
-
descriptions and explanations necessary for the understanding of the
drawings and diagrams and the operation of the product,
-
a list of the standards referred to in Schedule I, paragraph 2, applied in
full or in part, and descriptions of the solutions adopted to meet the
essential requirements of these regulations where the standards referred
to in Schedule I, have not been applied,
-
results of design calculations made, examinations carried out, etc.,
-
test reports.
4. The notified body must
4.1. examine the technical documents, verify that the type has been
manufactured in conformity with those documents and identify the elements which
have been designed in accordance with the relevant provisions of the standards
referred to in paragraph 2 of Schedule I, as well as the components which have been
designed without applying the relevant provisions of those standards;
4.2. perform or have performed the appropriate examinations and necessary tests
to check whether, where the standards referred to in paragraph 2 of Schedule I have
not been applied, the solutions adopted by the manufacturer meet the essential
requirements of these regulations;
4.3. perform or have performed the appropriate examinations and necessary tests
to check whether, where the manufacturer has chosen to apply the relevant
standards, these have actually been applied;
4.4. agree with the applicant the location where the examinations and necessary
tests are to be carried out.
5. Where the type meets the relevant provisions of these regulations, the
notified body issues an EC type-examination certificate to the applicant. The
certificate contains the name and address of the manufacturer, the conclusion of the
examination and necessary data for identification of the approved type.
A list of the relevant parts of the technical documents is annexed to the certificate
and a copy kept by the notified body.
If the manufacturer or his authorized representative is refused a type certificate,
the notified body must provide detailed reasons for such refusal.
Provision must be made for an appeals procedure.
(IMPLEMENTING MEASURES)
6. The applicant informs the notified body that holds the technical documents
concerning the EC type-examination certificate of all modifications to the approved
appliance which must receive additional approval where such changes may affect the
conformity with the essential requirements or the prescribed conditions for use of
the product. This additional approval is given in the form of an addition to the
original EC type-examination certificate.
Each notified body must communicate to the other notified bodies the
relevant information concerning the EC type-examination certificates and additions
issued and withdrawn.
The other notified bodies may receive copies of the EC type-examination
certificates and/or their additions. The Annexes to the certificates must be kept at the
disposal of the other notified bodies.
The manufacturer or his authorized representative must keep with the
technical documents copies of EC type-examination certificates and their additions
for a period of at least 10 years after the last date of manufacture of the product
concerned.
Where neither the manufacturer nor his authorized representative is established in
Malta, the obligation to keep the technical documents available is the responsibility
of the person who places the product on the market.
Schedule III
Based on Annex IV of Directive 92/42/EC
CONFORMITY TO TYPE AND QUALITY ASSURANCE
Module C: Conformity to type
1. This module describes that part of the procedure whereby the manufacturer
or his authorized representative ensures and declares that the appliances concerned
are in conformity with the type as described in the EC type-examination certificate
a nd s a t is f y t h e re qu ir e me nt s of th e s e r e g ul a t i on s th a t a pp ly to t h e m . T he
manufacturer or his authorized representative shall affix the CE marking to each
appliance and draw up a written declaration of conformity.
2. The manufacturer must take all measures necessary to ensure that the
manufacturing process assures the conformity of the manufactured appliances with
the type as described in the EC type-examination certificate and with the efficiency
requirements of the regulations.
3. The manufacturer or his authorized representative must keep a copy of the
declaration of conformity for a period of at least 10 years after the last date of
manufacture of the product concerned.
Where neither the manufacturer nor his authorized representative is established in
Malta, the obligation to keep the technical documents available is the responsibility
of the person who places the product on the market.
4. A notified body chosen by the manufacturer must perform or have
performed examinations of the product at random intervals. A suitable sample of the
finished products, taken on the spot by the notified body, is examined and
appropriate tests, defined in the applicable standard or standards referred to in
Schedule I, paragraph 2, or equivalent tests are carried out to check the conformity
(IMPLEMENTING MEASURES)
of the product with the requirements of the corresponding directive. In the event of
one or more samples of the products examined not conforming, the notified body
must take the appropriate measures.
Module D: Production quality assurance
1. This module describes the procedure whereby the manufacturer who
satisfies the obligations of section 2 of this Module, ensures and declares that the
appliances concerned are in conformity with the type as described in the EC type
examination certificate and satisfy the requirements of these regulations. The
manufacturer or his authorized representative shall affix the CE marking to each
appliance and draw up a written declaration of conformity. The CE marking is
accompanied by the identification number of the notified body responsible for the
checks referred to in section 4 of this Module.
2. The manufacturer must operate an approved quality system for production,
final appliance inspection and testing as specified in section 3 of this Module. He is
subject to the checks referred to in section 4 of this Module.
3. Quality system
3.1. The manufacturer lodges an application for assessment of his quality system
with a notified body of his choice, for the appliances concerned.
The application must include
-
all relevant information for the appliance category envisaged,
-
the documents concerning the quality system,
-
the technical documents pertaining to the approved type and a copy of
the EC type-examination certificate.
3.2. The quality system must ensure conformity of appliances with the type as
described in the EC type-examination certificate and with the requirements of these
regulations that apply to them.
All the elements, requirements and provisions adopted by the manufacturer must
be documented in a systematic and orderly manner in the form of written policies,
procedures and instructions. The quality system documents must permit a consistent
interpretation of the quality programmes, plans, manuals and quality records.
It must contain in particular an adequate description of
-
the quality objectives and the organizational structure, responsibilities
and powers of the management with regard to appliance quality,
-
the manufacturing, quality control and quality assurance techniques,
processes and systematic actions that will be used,
-
the examinations and tests that will be carried out before, during and
after manufacture, and the frequency with which they will be carried
out,
-
the quality records, such as inspection reports and test data, calibration
data, qualification reports of the personnel concerned, etc.,
-
the means of monitoring the achievement of the required appliance
quality and the effective operation of the quality system.
3.3. The notified body must assess the quality system to determine whether it
satisfies the requirements referred to in point 3.2 of this Module. It must presume
conformity with those requirements in respect of quality systems that implement the
(IMPLEMENTING MEASURES)
relevant harmonized standard. The auditing team must have at least one member
with experience of assessing the relevant product technology.
The assessment procedure includes an inspection visit to the manufacturer ’s
premises.
The decision is notified to the manufacturer. The notification must contain the
conclusions of the examination and the duly substantiated assessment decision.
3.4. The manufacturer must undertake to fulfil the obligations arising out of the
quality system as approved and maintain it at an adequate and efficient level.
The manufacturer or his authorized representative must keep the notified body
that has approved the quality system informed of any proposed change in the quality
system.
The notified body must assess the changes proposed and decide whether the
altered quality system will still satisfy the requirements referred to in point 3.2 of
this Module or whether reassessment is required.
It must notify the manufacturer of its decision. The notification must contain the
conclusions of the examination and the substantiated assessment decision.
4. Monitoring under the responsibility of the notified body
4.1. The purpose of monitoring is to make sure that the manufacturer duly fulfils
the obligations arising out of the approved quality system.
4.2. The manufacturer must allow the notified body access for inspection
purposes to the manufacturing, inspection, testing and storage premises and provide
it with all necessary information, in particular
-
the quality system documents,
-
the quality records, such as inspection reports and test data, calibration
data, qualification reports of the personnel concerned, etc..
4.3. The notified body must periodically carry out audits to make sure that the
manufacturer maintains and applies the quality system and provides an audit report
to the manufacturer.
4.4. Additionally the notified body may pay unannounced visits to the
manufacturer.
During such visits the notified body may carry out tests or have them carried out
to verify that the quality system is functioning correctly; if necessary, the notified
body must provide the manufacturer with a visit report and, if a test has taken place,
with a test report.
5. The manufacturer must, for a period of at least 10 years after the last date of
manufacture of the product, keep at the disposal of the national authorities
-
the document referred to in the second indent of point 3.1 of this
Module,
-
the updating referred to in the second paragraph of point 3.4 of this
Module,
-
the decisions and reports from the notified body which are referred to in
the final paragraph of point 3.4, and in point 4.3 and point 4.4 of this
Module.
6. Each notified body must give the other notified bodies the relevant
information concerning the quality system approvals issued and withdrawn.
(IMPLEMENTING MEASURES)
Module E: Product quality assurance
1. This module describes the procedure whereby the manufacturer who
satisfies the obligations of section 2 of this Module ensures and declares that the
boilers and appliances are in conformity with the type as described in the EC type
examination certificate.
The manufacturer or his authorized representative shall affix the CE marking to
each boiler and appliance and draw up a written declaration of conformity.
The CE marking must be accompanied by the identification number of the notified
body responsible for the checks referred to in section 4 of this Module.
2. The manufacturer must operate an approved quality system for final boiler
and appliance inspection and testing as specified in section 3 of this Module. He
must be subject to the checks referred to in section 4 of this Module.
3. Quality system
3.1. The manufacturer lodges an application with a notified body of this choice
for the assessment of the quality system for his boilers and appliances.
The application must include
-
all relevant information for the boiler or appliance category envisaged,
-
the quality system’s documentation,
-
the technical documents pertaining to the approved type and a copy of
the EC type-examination certificate.
3.2. Under the quality system, each boiler or appliance is examined and
appropriate tests as defined in the relevant standard(s) referred to in out in Schedule
I, or equivalent tests are carried out in order to verify its conformity with the
relevant requirements of these regulations. All the elements, requirements and
provisions adopted by the manufacturer must be documented in a systematic and
orderly manner in the form of written policies, procedures and instructions.
This quality system documentation must enable the quality programmes, plans,
manuals and records to be interpreted in a uniform manner.
It must in particular contain an adequate description of
-
the quality objectives and the organizational structure, responsibilities
and powers of the management with regard to product quality,
-
the examination and tests that will be carried out after manufacture, -
the means of monitoring the effective operation of the quality system,
-
quality records, such as inspection reports and test data, calibration
data, qualification reports of the personnel concerned, etc.
3.3. The notified body must assess the quality system to determine whether it
satisfies the requirements referred to in point 3.2 of this Module. It must presume
conformity with these requirements in respect of quality systems that implement the
relevant harmonized standard.
The auditing team must have at least one member with experience of assessing the
relevant product technology. The assessment procedure must include an inspection
visit to the manufacturer’s premises.
The manufacturer must be notified of the decision. The notification must contain
the conclusions of the examination and the substantiated assessment decision.
(IMPLEMENTING MEASURES)
3.4. The manufacturer must undertake to fulfil the obligations arising out of the
quality system as approved and maintain it at an adequate and efficient level.
The manufacturer or his authorized representative must keep the notified body
which has approved the quality system informed of any proposed change in the
quality system.
The notified body must assess the changes proposed and decide whether the
altered quality system will still satisfy the requirements referred to in section 3.2 of
this Schedule or whether a reassessment is required.
It must notify the manufacturer of its decision. The notification must contain the
conclusions of the examination and the substantiated assessment decision.
4. Monitoring under the responsibility of the notified body
4.1. The purpose of monitoring is to make sure that the manufacturer duly fulfils
the obligations arising out of the approved quality system.
4.2. The manufacturer must allow the notified body access for inspection
purposes to the inspection, testing and storage premises and provide it with all
necessary information, in particular
-
the quality system documentation,
-
the technical documents,
-
the quality records, such as inspection reports and test data, calibration
data, qualification reports of the personnel concerned, etc.
4.3. The notified body must periodically carry out audits to ensure that the
manufacturer maintains and applies the quality system and must provide an audit
report to the manufacturer.
4.4. Additionally, the notified body may pay unannounced visits to the
manufacturer.
During such visits the notified body may carry out tests or have them carried out
to verify that the quality system is functioning correctly; if necessary, the notified
body must provide the manufacturer with a visit report and, if a test has been carried
out, with a test report.
5. The manufacturer must, for a period of at least 10 years after the last date of
manufacture of the boiler or appliance, keep at the disposal of the national
authorities
-
the documents referred to in the third indent of point 3.1 of this Module,
-
the changes referred to in the second paragraph of point 3.4 of this
Module,
-
the decisions and reports from the notified body which are referred to in
the final paragraph of point 3.4, and in point 4.3 and point 4.4 of this
Module.
6. Each notified body must forward to the other notified bodies the relevant
information concerning the quality system approvals issued and withdrawn.
(IMPLEMENTING MEASURES)
Schedule IV
Based on Annex V of Directive 92/42/EC
MINIMUM CRITERIA TO BE TAKEN INTO ACCOUNT FOR THE
NOTIFICATION OF BODIES
1. The body, its director and the staff responsible for carrying out the
verification tests may not be the designer, manufacturer, supplier or installer of
appliances which they inspect, nor the authorized representative of any of those
parties. They may not become either involved directly or as authorized
representatives in the design, construction, marketing or maintenance of such boilers
and appliances. This does not preclude the possibility of exchanges of technical
information between the manufacturer and the body.
2. The body and its staff must carry out the verification tests with the highest
degree of professional integrity and technical competence and must be free from all
pressures and inducements, particularly financial, which might influence their
judgment of the results of the inspection, especially from persons or groups of
persons with an interest in the result of verifications.
3. The body must have at its disposal the necessary staff and possess the
necessary facilities to enable it to perform properly the administrative and technical
tasks connected with verification; it must also have access to the equipment required
for special verification.
4. The staff responsible for inspection must have
-
sound technical and professional training,
-
satisfactory knowledge of the requirements of the tests they carry out
and adequate experience of such tests,
-
the ability to draw up the certificates, records and reports required to
authenticate the performance of the tests.
5. The impartiality of inspection staff must be guaranteed. Their remuneration
must not depend on the number of tests carried out or on the results of such tests.
6. The body must take out liability insurance unless its liability is assumed by
the State in accordance with national law, or the Member State itself is directly
responsible for the tests.
7. The staff of the body must be bound to observe professional secrecy (except
vis-à-vis the competent administrative authorities of the State in which its activities
are carried out) under these regulations or any provision of national law giving effect
to it.